Peter Devilee


Ontology type: schema:Person     


Person Info

NAME

Peter

SURNAME

Devilee

Publications in SciGraph latest 50 shown

  • 2019-01 Clinicians’ use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey in JOURNAL OF COMMUNITY GENETICS
  • 2018-12 E-cadherin breast tumor expression, risk factors and survival: Pooled analysis of 5,933 cases from 12 studies in the Breast Cancer Association Consortium in SCIENTIFIC REPORTS
  • 2018-07-10 The functional impact of variants of uncertain significance in BRCA2 in GENETICS IN MEDICINE
  • 2018-07 Corrections to: Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries in FAMILIAL CANCER
  • 2018-07 A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer in NATURE GENETICS
  • 2018-06 The association between cancer family history and ovarian cancer risk in BRCA1/2 mutation carriers: can it be explained by the mutation position? in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2018-01 Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries in FAMILIAL CANCER
  • 2017-12 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-11 Association analysis identifies 65 new breast cancer risk loci in NATURE
  • 2017-06 Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk in NATURE GENETICS
  • 2017-05 Genetic modifiers of CHEK2*1100delC-associated breast cancer risk in GENETICS IN MEDICINE
  • 2016-12 Making sense of big data in health research: Towards an EU action plan in GENOME MEDICINE
  • 2016-12 Erratum to: Making sense of big data in health research: towards an EU action plan in GENOME MEDICINE
  • 2016-12 Genetic predisposition to ductal carcinoma in situ of the breast in BREAST CANCER RESEARCH
  • 2016-12 Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus in BREAST CANCER RESEARCH
  • 2016-12 Prognostic value of automated KI67 scoring in breast cancer: a centralised evaluation of 8088 patients from 10 study groups in BREAST CANCER RESEARCH
  • 2016-10 Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs) in SCIENTIFIC REPORTS
  • 2016-09-07 Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus in NATURE COMMUNICATIONS
  • 2016-07 Combined mismatch repair and POLE/POLD1 defects explain unresolved suspected Lynch syndrome cancers in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-04-27 Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer in NATURE COMMUNICATIONS
  • 2016-04 Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 in NATURE GENETICS
  • 2015-12 An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2015-12 Common germline polymorphisms associated with breast cancer-specific survival in BREAST CANCER RESEARCH
  • 2015-11 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair in NATURE GENETICS
  • 2015-06 High-resolution melting (HRM) re-analysis of a polyposis patients cohort reveals previously undetected heterozygous and mosaic APC gene mutations in FAMILIAL CANCER
  • 2015-04 Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer in NATURE GENETICS
  • 2014-12 2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy in NATURE COMMUNICATIONS
  • 2014-12 Refined histopathological predictors of BRCA1 and BRCA2mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia in BREAST CANCER RESEARCH
  • 2014-12 Paraganglioma and pheochromocytoma upon maternal transmission of SDHDmutations in BMC MEDICAL GENETICS
  • 2014-12 Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation in NATURE COMMUNICATIONS
  • 2014-12 Nuclear receptor NR4A1 promotes breast cancer invasion and metastasis by activating TGF-β signalling in NATURE COMMUNICATIONS
  • 2014-10 Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche in NATURE
  • 2014-08 Survival and contralateral breast cancer in CHEK2 1100delC breast cancer patients: impact of adjuvant chemotherapy in BRITISH JOURNAL OF CANCER
  • 2014-02 FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium in BRITISH JOURNAL OF CANCER
  • 2014-01 CHEK2*1100delC homozygosity in the Netherlands—prevalence and risk of breast and lung cancer in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-06 COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration in BREAST CANCER RESEARCH
  • 2013-04 Large-scale genotyping identifies 41 new loci associated with breast cancer risk in NATURE GENETICS
  • 2013-04 Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer in NATURE GENETICS
  • 2012-07 MUTYH gene variants and breast cancer in a Dutch case–control study in BREAST CANCER RESEARCH AND TREATMENT
  • 2012-06 Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study in BRITISH JOURNAL OF CANCER
  • 2012-04 Prediction of BRCA2-association in hereditary breast carcinomas using array-CGH in BREAST CANCER RESEARCH AND TREATMENT
  • 2012-03 Genome-wide association analysis identifies three new breast cancer susceptibility loci in NATURE GENETICS
  • 2011-11 A non-BRCA1/2 hereditary breast cancer sub-group defined by aCGH profiling of genetically related patients in BREAST CANCER RESEARCH AND TREATMENT
  • 2011-08 Allele-specific regulation of FGFR2 expression is cell type-dependent and may increase breast cancer risk through a paracrine stimulus involving FGF10 in BREAST CANCER RESEARCH
  • 2010-12 Increased MUTYH mutation frequency among Dutch families with breast cancer and colorectal cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2010-10 Subtypes of familial breast tumours revealed by expression and copy number profiling in BREAST CANCER RESEARCH AND TREATMENT
  • 2010-10 A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population in NATURE GENETICS
  • 2010-01 The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational family in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-12 A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an example in BMC CANCER
  • 2009-12 The first Dutch SDHB founder deletion in paraganglioma – pheochromocytoma patients in BMC MEDICAL GENETICS
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